Kunz WS - Search Results

1

Effect of coenzyme Q10 on the mitochondrial function of skin fibroblasts from Parkinson patients.

Winkler-Stuck K, Wiedemann FR, Wallesch CW, Kunz WS. Winkler-Stuck K, et al. Among authors: kunz ws. J Neurol Sci. 2004 May 15;220(1-2):41-8. doi: 10.1016/j.jns.2004.02.003. J Neurol Sci. 2004. PMID: 15140604

2

Is there mitochondrial dysfunction in amyotrophic lateral sclerosis skeletal muscle?

Vielhaber S, Kudin A, Winkler K, Wiedemann F, Schröder R, Feistner H, Heinze HJ, Elger CE, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Ann Neurol. 2003 May;53(5):686-7; author reply 687-8. doi: 10.1002/ana.10564. Ann Neurol. 2003. PMID: 12731009 No abstract available.

3

Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy.

Vielhaber S, Niessen HG, Debska-Vielhaber G, Kudin AP, Wellmer J, Kaufmann J, Schönfeld MA, Fendrich R, Willker W, Leibfritz D, Schramm J, Elger CE, Heinze HJ, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Epilepsia. 2008 Jan;49(1):40-50. doi: 10.1111/j.1528-1167.2007.01280.x. Epub 2007 Sep 5. Epilepsia. 2008. PMID: 17822430 Free article.

4

Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis.

Niessen HG, Debska-Vielhaber G, Sander K, Angenstein F, Ludolph AC, Hilfert L, Willker W, Leibfritz D, Heinze HJ, Kunz WS, Vielhaber S. Niessen HG, et al. Among authors: kunz ws. Eur J Neurosci. 2007 Mar;25(6):1669-77. doi: 10.1111/j.1460-9568.2007.05415.x. Eur J Neurosci. 2007. PMID: 17432958

5

Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6.

Hoepken HH, Gispert S, Morales B, Wingerter O, Del Turco D, Mülsch A, Nussbaum RL, Müller K, Dröse S, Brandt U, Deller T, Wirth B, Kudin AP, Kunz WS, Auburger G. Hoepken HH, et al. Among authors: kunz ws. Neurobiol Dis. 2007 Feb;25(2):401-11. doi: 10.1016/j.nbd.2006.10.007. Epub 2006 Nov 30. Neurobiol Dis. 2007. PMID: 17141510

6

Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies--a comment.

Vielhaber S, Kornblum C, Heinze HJ, Elger CE, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Brain. 2005 Dec;128(Pt 12):E38. doi: 10.1093/brain/awh652. Brain. 2005. PMID: 16311266 No abstract available.

7

Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.

Vielhaber S, Varlamov DA, Kudina TA, Schröder R, Kappes-Horn K, Elger CE, Seibel M, Seibel P, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. J Neuropathol Exp Neurol. 2002 Oct;61(10):885-95. doi: 10.1093/jnen/61.10.885. J Neuropathol Exp Neurol. 2002. PMID: 12387454

8

Mitochondrial dysfunction in myofibrillar myopathy.

Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schröder R. Reimann J, et al. Among authors: kunz ws. Neuropathol Appl Neurobiol. 2003 Feb;29(1):45-51. doi: 10.1046/j.1365-2990.2003.00428.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581339

9

Functional imaging of mitochondrial redox state.

Kunz D, Winkler K, Elger CE, Kunz WS. Kunz D, et al. Among authors: kunz ws. Methods Enzymol. 2002;352:135-50. doi: 10.1016/s0076-6879(02)52014-0. Methods Enzymol. 2002. PMID: 12125342 No abstract available.

10

In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient.

Niessen HG, Angenstein F, Sander K, Kunz WS, Teuchert M, Ludolph AC, Heinze HJ, Scheich H, Vielhaber S. Niessen HG, et al. Among authors: kunz ws. Exp Neurol. 2006 Oct;201(2):293-300. doi: 10.1016/j.expneurol.2006.04.007. Epub 2006 Jun 5. Exp Neurol. 2006. PMID: 16740261

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